A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525677



Internal ID15452970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102698199..102795157hg38UCSC Ensembl
Innerchr6:103146074..103243032hg19UCSC Ensembl
Innerchr6:103252767..103349725hg18UCSC Ensembl
Innerchr6:103252767..103349725hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3896959
hg1996959
hg1896959
hg1796959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701834
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525677
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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